PROCESS CONSIDERATIONS IN REDUCING TABLET FRIABILITY AND THEIR EFFECT ON IN-VITRO DISSOLUTION

被引:15
作者
GORDON, MS
机构
[1] Institute of Pharmaceutical Sciences Syntex (USA) Inc., Palo Alto, CA, 94304
关键词
D O I
10.3109/03639049409047211
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The tablet friability resulting from manufacturing process variations was studied for two differently sized tablets using the same formulation. Granulations containing lower moisture contents required higher compression and ejection forces to manufacture a tablet at a given hardness, although this did not influence friability. Increased tablet hardness (and to a lesser extent decreased tablet thickness) decreased the tablet friability of the larger tablet. An increase in the quantity of granulating fluid increased the granulation particle size and slightly improved compactibility without significantly affecting friability. Tablet dissolution increased as the quantity of granulating fluid was decreased. There was a strong interaction, with respect to dissolution, between moisture content and the amount of granulating fluid. Tablet hardness did not significantly influence dissolution. Doubling the quantity of magnesium stearate in the granulation in one tablet strength decreased the maximum tablet hardness that could be obtained, and for the other tablet strength increased friability. It also resulted in slower tablet dissolution.
引用
收藏
页码:11 / 29
页数:19
相关论文
共 10 条
[1]  
Carr R.L., 1965, CHEM ENG J, V72, P163
[2]  
CHOWHAN Z T, 1984, International Journal of Pharmaceutical Technology and Product Manufacture, V5, P6
[3]   EFFECT OF MOISTURE AND CRUSHING STRENGTH ON TABLET FRIABILITY AND INVITRO DISSOLUTION [J].
CHOWHAN, ZT ;
YANG, IC ;
AMARO, AA ;
CHI, LH .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1982, 71 (12) :1371-1375
[4]   PUNCH GEOMETRY AND FORMULATION CONSIDERATIONS IN REDUCING TABLET FRIABILITY AND THEIR EFFECT ON INVITRO DISSOLUTION [J].
CHOWHAN, ZT ;
AMARO, AA ;
ONG, JTH .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1992, 81 (03) :290-294
[5]   EFFECT OF INTERGRANULAR VERSUS INTRAGRANULAR CORNSTARCH ON TABLET FRIABILITY AND INVITRO DISSOLUTION [J].
CHOWHAN, ZT ;
YANG, IC .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (09) :983-988
[6]   OPTIMIZATION OF TABLET FRIABILITY, MAXIMUM ATTAINABLE CRUSHING STRENGTH, WEIGHT VARIATION AND INVITRO DISSOLUTION BY ESTABLISHING IN-PROCESS VARIABLE CONTROLS [J].
CHOWHAN, ZT ;
AMARO, AA .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1988, 14 (08) :1079-1106
[7]   EFFECT OF THE MODE OF CROSCARMELLOSE SODIUM-INCORPORATION ON TABLET DISSOLUTION AND FRIABILITY [J].
GORDON, MS ;
CHATTERJEE, B ;
CHOWHAN, ZT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (01) :43-47
[8]   OPTIMIZING THE FRIABILITY OF A TABLET FORMULATION [J].
LINDBERG, NO ;
HOLMQUIST, B .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1987, 13 (06) :1063-1067
[9]   EFFECTS OF BINDERS AND MOISTURE-CONTENT ON THE DISINTEGRATION, HARDNESS AND FRIABILITY OF PARACETAMOL AND ORPHENADRINE CITRATE TABLETS [J].
MUTI, H ;
OTHMAN, S .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1989, 15 (12) :2017-2035
[10]  
SHAFER EGE, 1956, J AM PHARM ASS SC ED, V40, P114